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TFG Gene SPG57 Genetic Test

Original price was: $700.Current price is: $500.

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The TFG Gene SPG57 NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the TFG gene associated with hereditary spastic paraplegia type 57 (SPG57). This comprehensive test utilizes next-generation sequencing technology to detect genetic variations that cause progressive neurological disorders characterized by muscle stiffness, weakness in the legs, and mobility challenges. The test is particularly valuable for individuals experiencing symptoms of spastic paraplegia or those with a family history of neurological conditions. Results provide crucial information for accurate diagnosis, treatment planning, and genetic counseling. The test is available for $500 USD (discounted from $700) and requires a simple blood sample or extracted DNA. Turnaround time is 3-4 weeks, and genetic counseling is recommended before testing.

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TFG Gene SPG57 NGS Genetic DNA Test

Comprehensive Genetic Testing for Hereditary Spastic Paraplegia

The TFG Gene SPG57 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise detection of mutations associated with hereditary spastic paraplegia type 57. This advanced testing methodology provides crucial insights for patients and healthcare providers dealing with complex neurological conditions.

What is the TFG Gene SPG57 Test?

The TFG (TRK-Fused Gene) gene plays a critical role in protein trafficking and endoplasmic reticulum function within nerve cells. Mutations in this gene are directly linked to SPG57, a specific form of hereditary spastic paraplegia characterized by progressive lower limb weakness and spasticity. Our NGS (Next-Generation Sequencing) technology enables comprehensive analysis of the entire TFG gene, identifying even subtle genetic variations that conventional methods might miss.

What Does This Test Detect?

This sophisticated genetic analysis specifically targets:

  • Point mutations, deletions, and insertions in the TFG gene
  • Autosomal recessive inheritance patterns associated with SPG57
  • Genetic variants affecting protein transport mechanisms in neurons
  • Mutations leading to impaired axonal transport and neurodegeneration
  • Specific genetic markers correlating with disease severity and progression

Who Should Consider TFG Gene SPG57 Testing?

Clinical Indications and Symptoms

This test is particularly recommended for individuals experiencing:

  • Progressive stiffness and weakness in the legs
  • Difficulty walking or changes in gait pattern
  • Muscle spasticity that worsens over time
  • Family history of hereditary spastic paraplegia
  • Early-onset neurological symptoms in childhood or adolescence
  • Unexplained lower limb hyperreflexia and extensor plantar responses
  • Bladder dysfunction associated with spastic paraplegia

Key Benefits of TFG Gene SPG57 Testing

Undergoing this comprehensive genetic analysis provides numerous advantages:

  • Accurate Diagnosis: Confirms or rules out SPG57 with high precision
  • Family Planning Guidance: Provides essential information for genetic counseling
  • Treatment Planning: Enables targeted therapeutic approaches
  • Prognostic Information: Helps predict disease progression and severity
  • Early Intervention: Facilitates timely management strategies
  • Research Contribution: Advances understanding of hereditary neurological disorders

Understanding Your Test Results

Interpretation Guidelines

Your TFG Gene SPG57 test results will fall into one of several categories:

  • Positive Result: Indicates the presence of pathogenic mutations confirming SPG57 diagnosis
  • Negative Result: No disease-causing mutations detected, though other genetic causes may need investigation
  • Variant of Uncertain Significance (VUS): Genetic changes with unclear clinical impact requiring further evaluation
  • Carrier Status: Identification of individuals carrying one copy of mutated gene without disease symptoms

All results are accompanied by detailed interpretation from our board-certified genetic specialists and recommendations for next steps in clinical management.

Test Pricing and Details

Test Component Details
Test Name TFG Gene SPG57 NGS Genetic DNA Test
Discount Price $500 USD
Regular Price $700 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Testing Method Next-Generation Sequencing (NGS) Technology

Pre-Test Requirements

To ensure optimal testing outcomes, we recommend:

  • Comprehensive clinical history documentation
  • Genetic counseling session to create detailed family pedigree
  • Discussion of testing implications with healthcare provider
  • Understanding of potential results and their impact

Nationwide Accessibility

We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network of certified collection centers ensures accessible testing regardless of your location.

Take Control of Your Neurological Health

Don’t let uncertainty about hereditary spastic paraplegia affect your quality of life. The TFG Gene SPG57 NGS Genetic DNA Test provides the clarity needed for informed medical decisions and personalized care planning.

Ready to schedule your test? Contact our genetic specialists today at +1(267) 388-9828 or book your appointment online. Our team is available to answer your questions and guide you through the testing process with compassion and expertise.

Take the first step toward understanding your genetic health and accessing targeted treatment options. Early detection and accurate diagnosis can significantly improve long-term outcomes for individuals with hereditary neurological conditions.